AccessGUDID - DEVICE: ADVIA Centaur® Systems, ACS:180® Systems CKMB Calibrator (00630414124803)

GUDID

Device Identifier (DI) Information

Brand Name: ADVIA Centaur® Systems, ACS:180® Systems CKMB Calibrator
Version or Model: 10311570
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 672174000
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414124803
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: CK-MB - CENTAUR - CAL - 2x2x2mL

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
44694	Creatine kinase myocardial isoenzyme (CKMB) IVD, calibrator	A material which is used to establish known points of reference for an assay intended to be used for the qualitative and/or quantitative detection of creatine kinase myocardial isoenzyme (CKMB) in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JHS	DIFFERENTIAL RATE KINETIC METHOD, CPK OR ISOENZYMES

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K962126	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Store Upright, Protect from Light, Do not freeze, Resuspend.
Storage Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 85d6d769-5d97-4e5d-8d22-d297c84d9095
Public Version Date: November 18, 2021
Public Version Number: 5
DI Record Publish Date: September 24, 2016